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使用空间位阻配体合成和光物理性质的单核 C^C* 铂(II)甲脒配合物。

Synthesis and Photophysical Properties of Monometallic C^C* Platinum(II) Formamidinate Complexes using Sterically Demanding Ligands.

机构信息

Physikalische Organische Chemie, Technische Universität Dresden, 01069, Dresden, Germany.

出版信息

Angew Chem Int Ed Engl. 2023 May 22;62(22):e202301225. doi: 10.1002/anie.202301225. Epub 2023 Apr 25.

Abstract

A novel class of cyclometalated platinum(II) complexes-previously considered to be inaccessible-was synthesized by an improved synthetic route utilizing ligands predicted by density functional theory calculations. Based on a concise quantum chemical screening three model ligands with varying steric demand were chosen and a series of six photoluminescent C^C* cyclometalated platinum(II) formamidinate complexes was obtained. The least sterically demanding ligand led to a bimetallic complex in two isomeric forms, which could be separated and confirmed by the corresponding solid-state structures. Sterically more hindered amidinate ligands gave the monometallic complexes supporting the theoretical predictions. The monometallic complexes show a significant hypsochromic shift of the emission wavelength, explained by the loss of the metal-metal interactions. Depending on the cyclometalating ligand quantum yields up to 87 % with short decay times were found for this new class of phosphorescent green-blue to pure blue platinum(II) emitters.

摘要

一种新型的环金属化铂(II)配合物——以前被认为是无法获得的——通过利用密度泛函理论计算预测的配体的改进合成路线合成。基于简洁的量子化学筛选,选择了三个具有不同空间位阻的模型配体,并获得了一系列六种光致发光的 C^C*环金属化铂(II)甲酰胺配合物。空间位阻最小的配体导致了两种异构形式的双金属配合物,这可以通过相应的固态结构来分离和确认。空间位阻更大的酰胺配体则提供了单核配合物,这支持了理论预测。单核配合物表现出发射波长的显著红移,这可以通过金属-金属相互作用的损失来解释。对于这种新型的磷光绿-蓝到纯蓝铂(II)发射体,根据环金属化配体的量子产率,发现高达 87%的量子产率具有短衰减时间。

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